EP4452301A1 - Peptide de collagène de type i à usage thérapeutique - Google Patents

Peptide de collagène de type i à usage thérapeutique

Info

Publication number
EP4452301A1
EP4452301A1 EP22844043.4A EP22844043A EP4452301A1 EP 4452301 A1 EP4452301 A1 EP 4452301A1 EP 22844043 A EP22844043 A EP 22844043A EP 4452301 A1 EP4452301 A1 EP 4452301A1
Authority
EP
European Patent Office
Prior art keywords
collagen
type
kda
recombinant
peptide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP22844043.4A
Other languages
German (de)
English (en)
Inventor
Stephan Hausmanns
Hans-Ulrich Frech
Steffen Oesser
Martin Hahn
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gelita AG
Original Assignee
Gelita AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gelita AG filed Critical Gelita AG
Publication of EP4452301A1 publication Critical patent/EP4452301A1/fr
Pending legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/78—Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin or cold insoluble globulin [CIG]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/39—Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin, cold insoluble globulin [CIG]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders

Definitions

  • the present invention relates to a type I collagen, in particular a collagen peptide, for use in a therapeutic method for the oral therapy of inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases, of a human or animal body.
  • inflammatory diseases are caused by misdirected immune reactions, in particular autoimmune diseases.
  • autoimmune diseases are atopic dermatitis, neurodermatitis, psoriasis, rosacea and acne in the area of the skin and, in the area of the mucous membrane, in particular inflammation of the intestinal mucosa such as Crohn's disease or ulcerative colitis.
  • a frequently used therapy is the intake of anti-inflammatory drugs and immunosuppressants such as cortisone, which suppress the body's own defences.
  • immunosuppressants such as cortisone
  • the suppression of the defense mechanism of the immune system can also lead to many side effects, such as skin atrophy or pigment disorders in cortisone-based topical therapy for neurodermatitis.
  • Other treatment options include the use of drugs that directly affect the immune system, stem cell therapies, psychotherapy, ergotherapy and physiotherapy, and nutritional advice.
  • therapeutically induced immunosuppression can lead to protection of the affected organs, it may increase susceptibility to infection.
  • Stem cell therapy is an ethically and legally controversial option for treating autoimmune diseases and also poses health risks.
  • compositions and active substances for the treatment of inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases, in particular those which overcome the aforementioned problems.
  • pharmaceutical compositions and active ingredients that not only alleviate the suffering of the affected patients symptomatically, but also treat it causally, ie eliminate the cause of the disease and/or its symptoms.
  • the present invention is therefore based on the technical problem of providing agents, in particular active ingredients and compositions containing them with a therapeutic effect, and methods for treating skin and mucosal inflammation, in particular skin and mucosal inflammation caused by autoimmune diseases, which overcome the aforementioned disadvantages, in particular, which can be produced in a standardized, reliable and well-defined form, also on a larger industrial and cost-effective scale, and due to their biological effectiveness for use in a method for oral therapy of inflammatory skin and mucous membrane diseases of the human or animal body and / or for maintaining the health of the skin and mucous membranes.
  • the present invention solves the technical problem on which it is based by providing the teachings of the independent patent claims, in particular also the teachings of the preferred embodiments of the description and the dependent patent claims.
  • the present invention relates to a type I collagen for use in a therapeutic method for the oral therapy of inflammatory skin and mucosal diseases in a human or animal patient, in particular immunomodulated inflammatory skin and mucosal diseases, in particular diseases of the intestinal mucosa, the type I collagen has a molecular weight of at least 16 kDa.
  • the present invention relates in particular to a type I collagen for use in a therapeutic method for the oral therapy of inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases, of a human or animal patient, the type I collagen having a molecular weight of at least 16 kDa and wherein the type I collagen is in the form of a natural or recombinant type I collagen.
  • the present invention is based on the surprising teaching that a recombinant or natural type I collagen, especially in isolated form, is able to treat inflammatory skin and mucosal diseases after oral administration if this type I collagen has a molecular weight of at least 16 kDa.
  • the recombinant or natural type I collagens provided according to the invention with a molecular weight of at least 16 kDa are capable of treating inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases, in particular those that are immunomodulated.
  • type I collagens in particular type I collagen peptides, are provided for this use according to the invention.
  • the recombinant type I collagen provided in a preferred embodiment according to the invention in particular recombinant type I collagen peptide, is able to demonstrate a biological effectiveness, in particular one that is at least the same as type I collagen also obtained from natural sources according to the invention , ie natural type I collagen, has, in particular even improved biological effectiveness is provided.
  • the present invention enables inflammatory skin and mucosal diseases in human or animal patients due to the high biological effectiveness of the recombinant type I collagens, in particular type I collagen peptides, in very low doses, i.e. low concentrations of the recombinant type I to treat collagen, in particular type I collagen peptides.
  • the teaching of the present invention therefore advantageously provides a reproducible, biotechnologically producible recombinant type I collagen with a molecular weight of at least 16 kDa for the oral therapy of inflammatory skin and mucous membrane diseases, which can be produced in a standardized manner and is produced on an industrial scale can, and which can be produced without contamination in high purity and yield without the limitation of natural starting materials and characterized in particular because of its high biological effectiveness in that it can be used in small doses.
  • the present invention also relates to type I collagen, particularly type I collagen peptides, having a molecular weight of at least 16 kDa for inducing oral tolerance, particularly for inducing oral tolerance to endogenously present collagen, particularly endogenously present type I collagen, particularly in skin - Endogenous type I collagen present in or mucosal tissue, in particular in immunomodulated inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases.
  • the present invention relates in particular to type I collagen, in particular recombinant type I collagen peptides, and compositions comprising type I collagen peptides, in particular recombinant type I collagen peptides, having a molecular weight of at least 16 kDa for use in a method for the therapeutic treatment or therapeutic prevention of Immune intolerance to type I collagen, in particular by inducing immune tolerance to type I collagen, in particular in immunomodulated inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases.
  • the present invention also relates to type I collagen, in particular recombinant type I collagen peptides having a molecular weight of at least 16 kDa for use in a method of inducing immune tolerance to type I collagen, in particular a composition whose administration is used to induce oral Tolerance to type I collagen leads, in particular in immunomodulated inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases.
  • the natural and recombinant type I collagens used according to the invention are characterized by a biological activity that unfolds after oral administration in human or animal bodies, in particular an immune-modulating and/or inflammation-modulating effect biological effectiveness.
  • this biological activity is present in particular for natural and recombinant, preferably recombinant, type I collagens present in non-denatured, i.e. native, form, in a preferred embodiment also for recombinant type I collagen peptides.
  • type I collagens provided according to the invention are preferably capable of immunomodulation and/or induction of oral tolerance, in particular they bring about an immune response and/or induction of oral tolerance in the treated human or animal body .
  • the natural or recombinant type I collagens provided according to the invention with a molecular weight of at least 16 kDa preferably develop a biological activity that suppresses the synthesis of immunoglobulins and/or an anti-inflammatory biological activity. According to the invention, the reduction of pro-inflammatory and the stimulation of anti-inflammatory cytokines could be determined.
  • the natural or recombinant type I collagen provided according to the invention in particular recombinant type I collagen peptide, with a molecular weight of at least 16 kDa, which is orally applied, completely or largely undamaged the gastrointestinal Passage survives and triggers immune-modulating and/or cytokine-regulating reactions and/or signaling cascades in immunomodulating, in particular immunosuppressor cells, in particular cells of the Peyer's Plaque, which reduce or completely undesired immune reactions and inflammatory processes in the area of the skin and mucosa, in particular intestinal mucosa stop.
  • the oral administration provided according to the invention of natural or recombinant type I collagen, in particular type I collagen peptides, with a molecular weight of at least 16 kDa appears, without being bound to theory, to induce oral tolerance to endogenously present type I collagen that triggers such undesirable reactions.
  • type I collagen in particular type I collagen peptides
  • a molecular weight of at least 16 kDa appears, without being bound to theory, to induce oral tolerance to endogenously present type I collagen that triggers such undesirable reactions.
  • a therapy of inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases is made possible.
  • the recombinant or natural type I collagens provided according to the invention are preferably equipped with the ability to interact with cells of the treated human or animal patient, in particular with cells of the Peyer's eye plaque, and in particular to stimulate anti-inflammatory and to inhibit pro-inflammatory cytokines and to regenerate immunosuppressive M2 macrophages and T-suppressor cells.
  • the inflammatory and immunomodulated skin and mucous membrane diseases which can be treated particularly preferably according to the invention are diseases of the Skin, such as cutaneous lupus erythematosus, dermatomyositis, lichen sclerosus, neurodermatitis, psoriasis, rosacea, lichen planus, bullous pemphigoid, pemphigus vulgaris and acne or the mucosa, in particular the intestinal mucosa, such as Crohn's disease, celiac disease or ulcerative colitis.
  • diseases of the Skin such as cutaneous lupus erythematosus, dermatomyositis, lichen sclerosus, neurodermatitis, psoriasis, rosacea, lichen planus, bullous pemphigoid, pemphigus vulgaris and acne
  • the mucosa in particular the intestinal mucosa, such as Crohn's disease, celiac disease or ulcerative colitis
  • the present invention relates to a type I collagen, wherein the recombinant or natural collagen, in particular recombinant or natural type I collagen peptide, in an isolated, homogeneous form with a uniform molecular weight in a range of at least 16 kDa, in particular at least 20 kDa, or as an isolated collagen mixture, in particular collagen peptide mixture, each collagen, in particular collagen peptide, having a molecular weight of at least 16 kDa, in particular at least 20 kDa.
  • the type 1 collagen used according to the invention in particular recombinant or natural type I collagen, in particular type I collagen peptide, can therefore be exactly the same in one embodiment of the present invention in the form of a mixture with type 1 collagens, in particular type 1 collagen peptides Size and the same molecular weight, ie in a homogeneous form with a uniform molecular weight in a range of at least 16 kDa, in particular at least 20 kDa.
  • the type I collagen used according to the invention in particular recombinant or natural type 1 collagen, in particular type I collagen peptide, can be in the form of a mixture with other type 1 collagens, in particular type I collagen peptides have a different molecular weight, all type I collagens, in particular type I collagen peptides of the mixture, having a molecular weight of at least 16 kDa, in particular at least 20 kDa.
  • the recombinant or natural type I collagen used according to the invention in particular the type I collagen peptide, with a molecular weight of at least 16 kDa is free of collagen, in particular also free of collagen peptides, with a molecular weight of less than 16 kDa before.
  • the recombinant or natural type I collagen used according to the invention in particular the type I collagen peptide, with a molecular weight of at least 16 kDa is free of type I collagen, in particular also free of type I collagen peptides with a molecular weight of less than 16 kDa.
  • the recombinant or natural type I collagen can be present in the form of type I procollagen or mature type I collagen.
  • the recombinant or natural type I collagen can be in triple-helical form, in particular in the form of a heterotrimer of two type I-a1 chains and one type I-a2 chain.
  • the recombinant or natural type I collagen is present in non-denatured form, also referred to here as native form, ie it has the naturally occurring tertiary and quaternary protein structure.
  • the present invention provides a type I collagen which can be present in the form of a type I collagen peptide, ie in single-stranded form, or in multi-stranded, for example two- or three-stranded form, here also as triple helicals Designated form, in particular in the form of a type I procollagen or mature type I collagen, in particular in the form of a heterotrimer of type I a1 and type I a2 chains.
  • the natural or recombinant type I collagen according to the invention is not present as a single-stranded type I collagen peptide, but instead is present, for example, in a triple-helical form, one or all of the individual collagen peptides that construct the triple-helical form of type I collagen can be embodied in accordance with the present invention.
  • the statements made in the present teaching relating to recombinant or natural type I collagen peptides also apply to type I collagens which have one, two or three such single-stranded type I collagen peptides, in particular are completely composed of these, in particular of those according to the invention natural, preferably recombinant, type I collagen peptides.
  • the recombinant or natural type I collagen can be bovine type I collagen.
  • the recombinant or natural type I collagen can be type I-al or type I-a2 collagen, in particular type I-al.
  • the recombinant or recombinant type I collagen can be present in the form of crosslinked or non-crosslinked fibrils.
  • the recombinant or natural type I collagen in particular type I collagen peptide, can be a full-length collagen peptide, ie have the complete amino acid sequence of a naturally occurring type I collagen peptide.
  • the recombinant type I collagen is in the form of a recombinant type I collagen peptide, in particular of the type I-al.
  • the recombinant type I collagen, in particular type I collagen peptide is a type I collagen peptide having a molecular weight in the range from 16 to 400 Da, in particular 16 to 390 kDa, in particular 16 to 350 kDa, in particular 16 to 300 kDa, in particular 16 to 110 kDa, in particular 20 to 400 kDa, in particular 20 to 390 kDa, in particular 20 to 350 kDa, in particular 20 to 300 kDa, in particular 20 to 110 kDa, in particular 40 to 110 kDa, in particular 40 to 100 kDa, in particular 21 to 105 kDa, in particular 25 to 100 kDa, in particular 20 to 99 kDa, in particular 25 to 95 kDa, in particular 30 to 95 kDa, in particular 35 to 95 kDa.
  • the recombinant type I collagen in particular collagen peptide, preferably comprises a
  • the recombinant type I collagen in particular collagen peptide, preferably comprises a
  • the recombinant type I collagen in particular collagen peptide, preferably comprises a
  • the recombinant type I collagen in particular collagen peptide, preferably comprises a
  • the natural type I collagen in particular type I collagen peptide
  • the natural type I collagen preferably has a collagen peptide in particular
  • the natural type I collagen preferably has a collagen peptide in particular
  • the natural type I collagen preferably has a collagen peptide in particular
  • the natural type I collagen preferably has a collagen peptide in particular
  • the recombinant or natural type I collagen, in particular the recombinant or natural type I collagen peptide, of the present invention is fully or partially hydroxylated, fully or partially glycosylated, or fully or partially hydroxylated and glycosylated.
  • the recombinant or natural type I collagen in particular the recombinant or natural type I collagen peptide, according to the present invention is a non-hydroxylated type I collagen, in particular type I collagen peptide.
  • the recombinant or natural type I collagen in particular the recombinant or natural type I collagen peptide, according to the present invention is a hydroxylated type I collagen, in particular type I collagen peptide.
  • the recombinant or natural type I collagen in particular the recombinantly produced or natural type I collagen peptide, preferably has hydroxylated proline and/or hydroxylated lysine.
  • the recombinant or natural type I collagen, in particular the recombinant or natural type I collagen peptide is preferably a non-hydroxylated, partially hydroxylated or fully hydroxylated type I collagen, in particular type I collagen peptide.
  • the recombinant or natural type I collagen in particular the recombinant or natural type I collagen peptide
  • the recombinant or natural type I collagen, in particular the recombinant or natural type I collagen peptide is preferably glycosylated on at least one hydroxylated lysine.
  • any hydroxylated lysine of the recombinant or natural type I collagen, in particular the recombinant or natural type I collagen peptide is glycosylated.
  • the recombinant type I collagen in particular recombinant type I collagen peptide, has no amino acid modification, in particular no hydroxylation.
  • the recombinant type I collagen, in particular type I collagen peptide particularly preferably has no hydroxylated and/or glycosylated amino acids.
  • the type I collagen according to the invention in particular type I collagen peptide, preferably has a type I collagen from vertebrates, in particular from fish, amphibians, reptiles, birds and mammals, in particular in pigs, sheep, cattle, rodents, kangaroos, horses or from invertebrates, in particular jellyfish, occurring amino acid sequence, in particular an amino acid sequence occurring in type I collagen from bovine.
  • the type I collagen, in particular type I collagen peptide particularly preferably comprises the amino acid sequence as shown in SEQ ID No. 2, 4, 6 or 8.
  • the type I collagen, in particular type I collagen peptide preferably consists of the amino acid sequence as shown in SEQ ID No, 2, 4, 6 or 8.
  • the type I collagen in particular type I collagen peptide, has at least 80%, preferably at least 85%, preferably at least 90%, preferably at least 95%, preferably at least 96%, preferably at least 97% preferably at least 98%, preferably at least 99%, sequence identity with the amino acid sequence according to SEQ ID No. 2, 4, 6 or 8.
  • the amino acid sequence of the recombinant type I collagen, in particular type I collagen peptide is preferably the amino acid sequence of a naturally occurring type I collagen, especially type I collagen peptides.
  • the amino acid sequence of the recombinant type I collagen, especially type I collagen peptide is the amino acid sequence of a naturally non-occurring type I collagen, especially type I collagen peptide.
  • the amino acid sequence of the recombinant type I collagen, in particular type I collagen peptide is preferably the amino acid sequence of a genetically modified type I collagen, in particular type I collagen peptide.
  • the type I collagen according to the invention in particular type I collagen peptide, particularly preferably has an amino acid sequence occurring in non-human collagen, in particular in non-human type I collagen peptides, preferably in the a1 chain of non-human type I collagen , in particular an amino acid sequence occurring in bovine, porcine, equine, ovine, piscine or avian collagen, in particular an amino acid sequence occurring in bovine collagen.
  • the recombinant type I collagen in particular the recombinant type I collagen peptide, is collagenase-resistant, in particular resistant to digestion by human collagenases.
  • the recombinant or natural type I collagen, in particular type I collagen peptide, having a molecular weight of at least 16 kDa is capable of inducing oral tolerance, in particular against endogenously present collagen, in particular endogenously present Type I collagen, in particular endogenous type I collagen present in skin or mucous membranes.
  • the recombinant or natural type I collagen, in particular type I collagen peptide, having a molecular weight of at least 16 kDa is capable of suppressing the synthesis of immunoglobulins.
  • the recombinant or natural type I collagen, in particular type I collagen peptide, having a molecular weight of at least 16 kDa is capable of suppressing the synthesis of proinflammatory cytokines.
  • the recombinant or natural type I collagen in particular type I collagen peptide, with a Molecular weight of at least 16 kDa capable of stimulating the synthesis of anti-inflammatory cytokines.
  • the natural or recombinant type I collagens provided according to the invention in particular recombinant type I collagen peptides, preferably show an inducing effect on the differentiation of peripheral blood monocytes into immunosuppressive M2 macrophages.
  • the recombinant or natural type I collagens provided according to the invention lead to a reduction in the synthesis of pro-inflammatory cytokines, in particular TNF ⁇ and IFN ⁇ , and/or to an induction of the synthesis of anti-inflammatory ones Cytokines, especially IL-10, IL-4 and TGF-ß, especially IL-10.
  • the recombinant or natural type I collagens provided according to the invention stimulate/induce the differentiation of na ⁇ ve CD4+T progenitor cells into T suppressor cells.
  • the stimulation/induction of the differentiation of na ⁇ ve CD4+T progenitor cells into T suppressor cells particularly preferably leads to an increased release of anti-inflammatory cytokines, preferably IL-10, IL-4 and/or TGF- ⁇ .
  • the recombinant or natural type I collagens provided according to the invention bring about reduced expression of pro-inflammatory cytokines, preferably IL-1 ⁇ , IFNY, TNFa and/or IL-6 , particularly by dermal fibroblasts.
  • the recombinant or natural type I collagen, in particular type I collagen peptide, having a molecular weight of at least 16 kDa is capable of suppressing the synthesis of immunoglobulins, the synthesis of pro-inflammatory cytokines to suppress and stimulate the synthesis of anti-inflammatory cytokines.
  • the recombinant or natural type I collagen, in particular type I collagen peptide, for use in a therapeutic method for the oral therapy of inflammatory skin and Mucosal diseases of a human or animal patient have a molecular weight in a range from 16 to 400 kDa, in particular 16 to 390 kDa, in particular 16 to 350 kDa, in particular 16 to 300 kDa, in particular 16 to 110 kDa, in particular 20 to 400 kDa, in particular 20 to 390 kDa, in particular 20 to 350 kDa, in particular 20 to 300 kDa, in particular 20 to 110 kDa, in particular 40 to 110 kDa, in particular 40 to 100 kDa. in particular 21 to 105 kDa, in particular 25 to 100 kDa, in particular 20 to 99 kDa, in particular 25 to 95 kDa, in particular 30 to 95 kDa, in particular 35 to 95 kDa.
  • the recombinant or natural type I collagen, in particular type I collagen peptide, for use in a therapeutic method for the oral therapy of inflammatory skin and mucosal diseases in a human or animal patient has a molecular weight in the range of 35 to 95, in particular 40 to 92 kDa.
  • the recombinant or natural type I collagen, in particular collagen peptide preferably has a molecular weight in a range from 16 to 25 kDa, in particular 16 kDa.
  • the recombinant or natural type I collagen, in particular collagen peptide preferably has a molecular weight in a range from 20 to 50 kDa, in particular 20 kDa.
  • the recombinant or natural type I collagen preferably has a molecular weight in the range from 40 to 50 kDa, in particular 45 kDa.
  • the recombinant or natural type I collagen preferably has a molecular weight in a range from 80 to 100 kDa, in particular 92 kDa.
  • the recombinant or natural type I collagen according to the invention in particular type I collagen peptide, is used alone, i.e. in isolated form, ie without further substances, in particular without any further collagen, in the use provided according to the invention.
  • the recombinant or natural type I collagen according to the invention in particular type I collagen peptide, is present as a homogeneous preparation, in particular as a homogeneous preparation of a single recombinant or natural type I collagen, in particular type I collagen peptide, with a uniform Molecular weight of at least 16 kDa, in particular at least 20 kDa, in particular without any further collagen.
  • the recombinant or natural type I collagen according to the invention in particular type I collagen peptide, is a mixture of type I collagen, in particular type I collagen peptides, all of which have a molecular weight of at least 16 kDa, in particular at least 20 kDa , exhibit, in particular without any further collagen.
  • the recombinant or natural type I collagen according to the invention in particular type I collagen peptide, is used as the only substance having biological activity in the use provided according to the invention.
  • the present invention relates to compositions having at least one type I collagen peptide, in particular at least one type I collagen peptide peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, which, in addition to the at least one recombinant or natural type I Collagen, in particular the at least one recombinant or natural type I collagen peptide, and optionally a pharmaceutically acceptable and/or food-compatible carrier, contain no further substances, in particular without any further collagen.
  • the composition comprising at least one type I collagen peptide, in particular at least one type I collagen peptide peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, is in a dosage form suitable for oral administration in a human or animal body before.
  • the present invention also relates to a composition
  • a composition comprising at least one type I collagen peptide, in particular at least one type I collagen peptide, having a molecular weight of at least 16 kDa, in particular at least 20 kDa, according to the present invention and at least one pharmaceutically acceptable and/or food compatible Carrier and, optionally, at least one additive or adjuvant for use in a therapeutic method for the oral therapy of inflammatory skin and mucosal diseases.
  • the present invention therefore also relates to a composition for use in a method for the therapeutic prophylaxis or therapeutic treatment of immune intolerance reactions to type I collagen, in particular endogenous type I collagen, by inducing oral tolerance to type I collagen, in particular endogenous type I collagen.
  • the present invention also relates to a composition for use in a method for inducing oral tolerance to type I collagen, in particular endogenous type I collagen, which composition results in the induction of oral tolerance in the human or animal body.
  • the present invention also relates to a composition
  • a composition comprising type I collagen peptides, in particular recombinant or natural type I collagen peptides, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, in particular pharmaceutical compositions or dietary supplements, or food or luxury foods, for use for the induction of oral tolerance to type I collagen, particularly endogenous type I collagen.
  • compositions according to the invention for oral administration can be, in particular, pharmaceutical compositions, dietary supplements or foodstuffs and semi-luxury foods.
  • the compositions according to the invention are pharmaceutical compositions.
  • the compositions according to the invention are food supplements.
  • the present invention relates in particular to a pharmaceutical composition
  • a pharmaceutical composition comprising a type I collagen according to the invention, in particular type I collagen peptide, having a molecular weight of at least 16 kDa, in particular at least 20 kDa, and at least one pharmaceutically acceptable carrier, and the pharmaceutical composition for use in a method for the therapeutic treatment of inflammatory skin and mucous membrane diseases of the human or animal body.
  • the type I collagen according to the invention, in particular type I collagen peptide be administered in the form of a pharmaceutical composition.
  • the pharmaceutical composition according to the invention is particularly advantageously administered, for example, in the form of tablets, lozenges, chewable tablets, powder, granules, hard capsules, soft capsules, capsules, bite capsules, coated tablets, lozenges, extrudates, juices, suspensions, gels or ointments.
  • the type I collagen used according to the invention in particular type I collagen peptide, is present in a dosage form which enables delayed intestinal release, in particular sustained-release capsules.
  • the composition according to the invention is in a form suitable for oral administration, in particular at a dose of 1 to 60 mg/day, in particular 5 to 50 mg/day, type collagen, in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa,
  • the present invention further relates to a dietary supplement comprising a type I collagen according to the invention, in particular type I collagen peptide, having a molecular weight of at least 16 kDa, in particular at least 20 kDa, and at least one food-acceptable carrier, and the dietary supplement for use in a Process for the therapeutic treatment of inflammatory skin and mucous membrane diseases in the human or animal body.
  • a dietary supplement comprising a type I collagen according to the invention, in particular type I collagen peptide, having a molecular weight of at least 16 kDa, in particular at least 20 kDa, and at least one food-acceptable carrier, and the dietary supplement for use in a Process for the therapeutic treatment of inflammatory skin and mucous membrane diseases in the human or animal body.
  • the type I collagen according to the invention in particular type I collagen peptide, be administered in the form of a dietary supplement.
  • the food supplement according to the invention is particularly advantageously in the form of a hard capsule, soft capsule, capsule, bite capsule, tablet, coated tablet, lozenge, sachet, extrudate, solution, suspension or gel, for example in an ampoule, as granules or powder.
  • the invention also relates to a foodstuff or luxury food, comprising a type I collagen according to the invention, in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, and the food or luxury food for use in a method for therapeutic treatment of inflammatory skin and mucous membrane diseases of the human or animal body.
  • the food or luxury food is a chocolate bar, protein bar, cereal bar, instant powder for preparing drinks, milk, dairy products, for example yoghurt, whey or quark and milk substitutes, for example soy milk, rice milk, almond milk and coconut milk, functional food or a drink, for example a refreshing or fitness drink.
  • the recombinant type I collagen, in particular type I collagen peptide is not the only component of a composition that has biological activity, in particular a pharmaceutical Composition, a dietary supplement, or a food or luxury food, it can be combined with one or more other additives or auxiliaries, especially those that have a positive effect on general health, especially on the health of the skin and mucous membranes.
  • preferred excipients are selected from the group consisting of vitamin C, vitamins from the B, D, E and K series, omega-3 fatty acids, omega-6 fatty acids, conjugated linolenic acids, caffeine and its derivatives, guarana extract, rosehip extract, Green tea extract, polyphenols, epigallocatechin gallate, creatine, L-camitine, a-lipoic acid, N-acetylcysteine, NADH, D-ribose, magnesium aspartate, antioxidants such as anthocyanins, carotenoids, flavonoids, resveratrol, glutathione and superoxide dismutase, minerals such as iron, magnesium, calcium , zinc, selenium and phosphorus, as well as other proteins, hydrolysates and peptides such as soy, wheat and whey protein.
  • the composition according to the invention in particular the pharmaceutical composition, the dietary supplement or the food or semi-luxury food, has a corticosteroid, in particular a glucocorticoid, in particular cortisone.
  • the composition according to the invention in particular the pharmaceutical composition, the dietary supplement or a foodstuff, or luxury food, has an additive, the additive being a recombinantly produced collagen hydrolyzate, a collagen hydrolyzate originating from natural sources, a recombinantly produced type I collagen, a type I collagen obtained from a natural source or a combination thereof, in particular each having a molecular weight of at least 16 kDa, in particular at least 20 kDa.
  • the products according to the invention in particular the pharmaceutical composition, the dietary supplement, or the food or luxury food, contain no other proteins or peptides, in particular no other collagen peptides, in addition to the type I collagen according to the invention, in particular type I collagen peptide .
  • the present invention also relates to methods for therapy, in particular for the prevention and/or treatment of inflammatory skin and mucous membrane diseases, according to which the human or animal body is given a sufficient for the therapeutic purpose
  • Amount of at least one of the recombinant or natural type I collagens according to the invention, in particular type I collagen peptides, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, optionally with a carrier and, optionally, an adjuvant or additive, is administered orally.
  • the present invention also relates to methods for inducing oral tolerance to type I collagen, in particular endogenous type I collagen, in a human or animal body, comprising administering an amount sufficient for a therapeutic purpose of at least one of the recombinant or natural type I collagens according to the invention Collagens, in particular recombinant or natural type I collagen peptides, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, optionally using a carrier and, optionally, an adjuvant or additive, the administration being oral.
  • the present invention also relates to methods for the therapeutic treatment or therapeutic prophylaxis of immune intolerance to type I collagen, in particular type I collagen peptide, comprising the oral administration of an amount sufficient for a therapeutic purpose of at least one of the recombinant or natural type I collagens according to the invention, in particular recombinant or natural type I collagen peptides, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, optionally by means of a carrier and, optionally, an adjuvant or additive.
  • the present invention also relates to the use of recombinant or natural type I collagen, in particular recombinant or natural type I collagen peptides, having a molecular weight of at least 16 kDa, in particular at least 20 kDa, in non-therapeutic methods of maintaining human skin and mucosal health or animal, according to which the human or animal body is given a quantity of at least one of the recombinant or natural type I collagens according to the invention, in particular type I collagen peptides, which is sufficient to maintain the health of the skin and mucous membranes, optionally with a carrier and, optionally, an auxiliary or additive, is administered orally.
  • the human or animal does not have any skin or mucosal disease.
  • oral administration of recombinant or natural type I collagen, in particular recombinant type I collagen peptides, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, to a human or an animal may be provided which does not have a skin or mucosal disease and which maintains its skin and mucosal health, in particular intestinal mucosal health, through the administration of the natural or recombinant type I collagen, in particular recombinant or natural type I collagen peptide.
  • the present invention relates to a method for producing a recombinant type I collagen which can be used according to the invention, in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, comprising the method steps: a) providing an expression system which has at least one Has an expression cassette, wherein the expression cassette has at least one nucleotide sequence which encodes a type I collagen, in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, b) culturing the expression system under conditions which promote expression of type I collagen, in particular type I collagen peptide, and c) obtaining the type I collagen according to the invention, in particular type I collagen peptide, having a molecular weight of at least 16 kDa, in particular at least 20 kDa.
  • the process provided according to the invention for the production of a recombinant type I collagen which can be used according to the invention, in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, is characterized in particular by the fact that a precisely defined, recombinantly produced type I Collagen, in particular type I collagen peptide, is obtained, which, in particular because of its biological effectiveness, is suitable for use in a method for the therapeutic treatment of inflammatory skin and mucous membrane diseases in the human or animal body or for maintaining skin or mucous membrane health.
  • the recombinant type I collagen provided according to the invention in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, has, due to its recombinant production method, compared to, for example, hydrolytically obtained type I collagen, in particular type I- collagen peptides, a particularly high purity. It can be done in a variety of ways Also provide expression systems on an industrial scale without undesired contamination, the recombinant type I collagen, in particular type I collagen peptide, at the same time advantageously having a biological activity.
  • Type I collagen peptide and its production is described for example in WO 2005/012356, WO 01/34646, WO 01/34647 and WO 01/34801. These documents disclose the production of recombinant type I collagen peptides and the hydroxylation and fibrillogenesis for production of procollagen in recombinant cell culture and with regard to the production of recombinant type I collagen and recombinant type I collagen peptides, in particular in hydroxylated and triple-helical form , fully included in the present disclosure content.
  • the biological effectiveness found according to the invention of the recombinant type I collagen, in particular the type I collagen peptides, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, and associated with it or their suitability for use in a method for the therapeutic treatment of inflammatory skin - and mucosal diseases of the human or animal body in a preferred embodiment, the type I collagen, in particular type I collagen peptides, obtained directly from the method according to the invention advantageously already occurs without the need for further processing steps.
  • both the hydroxylated and the non-hydroxylated recombinant type I collagens, in particular type I collagen peptides, according to the present invention have a biological activity, in particular at least the same biological activity as type I collagen obtained from natural sources , particularly preferably better biological activity than type I collagen obtained from natural sources.
  • the recombinant type I collagens according to the invention in particular type I collagen peptides, surprisingly have a biological activity even in non-hydroxylated form, preferably the same biological activity as type I collagen obtained from natural sources, particularly preferably one better biological effectiveness than type I collagen derived from natural sources.
  • Both the hydroxylated and the non-hydroxylated recombinant type I collagens, in particular type I collagen peptides, according to the present invention preferably show a biological activity, preferably at least the same biological activity as from Type I collagen obtained from natural sources, particularly preferably a better biological activity such as Type I collagen obtained from natural sources.
  • the expression system provided in step a) is preferably a host cell, in particular a prokaryotic or eukaryotic cell.
  • the expression system is preferably a host cell selected from the group consisting of bacterial cell, yeast cell, fungal cell, mammalian cell, insect cell and plant cell.
  • the expression system in particular the host cell, is preferably a bacterial cell, in particular of the Escherichia coli or Bacillus subtilis species.
  • the expression system in particular the host cell, is a yeast cell, in particular of the species Saccharomyces cerevisiae, Komagataella phaffi or Ogataea angusta (Hansenula polymorpha), in particular Komagataella phaffi.
  • the expression system in particular the host cell, is preferably a fungal cell, in particular of the species Aspergillus niger.
  • the expression system in particular the host cell, is a mammalian cell, in particular a CHO cell, a HeLa cell or a HEK293 cell.
  • the expression system in particular the host cell, is preferably an insect cell, in particular an Sf-9, Sf-21 or Tn-5 cell.
  • the expression system in particular the host cell, is preferably a plant cell, in particular a maize or tobacco cell.
  • the expression system provided in step a) is a host cell capable of hydroxylating proline, lysine or proline and lysine residues of the expressed collagen peptide.
  • the expression system provided in step a) is preferably a host cell which is capable of hydroxylating proline, lysine or proline and lysine residues of the expressed collagen peptide.
  • the expression system provided in step a) is preferably an expression system which has prolyl hydroxylase and/or lysyl hydroxylase activity. This is preferred in step a) provided expression system a host cell having prolyl hydroxylase and / or lysyl hydroxylase activity.
  • the expression system provided in step a) is a host cell which has at least one expression cassette which comprises a prolyl-4-hydroxylase-encoding polynucleotide sequence.
  • the expression system provided in step a) is particularly preferably a host cell which has at least one expression cassette which comprises a prolyl-4-hydroxylase-encoding polynucleotide sequence, so that in method step c) an in vivo hydroxylated type I collagen, in particular type I collagen collagen peptide is obtained.
  • the expression system provided in step a) is a host cell which has at least one expression cassette which comprises a lysyl hydroxylase-encoding polynucleotide sequence.
  • the expression system provided in step a) is particularly preferably a host cell which has at least one expression cassette which comprises a lysyl hydroxylase-encoding polynucleotide sequence, so that in method step c) an in vivo hydroxylated type I collagen, in particular type I collagen peptide, is obtained .
  • the expression system provided in step a) is a host cell which has at least one expression cassette which comprises a prolyl-4-hydroxylase-encoding polynucleotide sequence and at least one expression cassette which comprises a lysyl-hydroxylase-encoding polynucleotide sequence.
  • the expression system provided in step a) is particularly preferably a host cell which has at least one expression cassette which comprises a prolyl-4-hydroxylase-encoding polynucleotide sequence and at least one expression cassette which comprises a lysyl-hydroxylase-encoding polynucleotide sequence, so that in method step c). in vivo hydroxylated type I collagen, in particular type I collagen peptide is obtained.
  • the present invention thus also relates to a method for producing a recombinant type I collagen which can be used according to the invention, in particular type I collagen peptide, in particular an in vivo hydroxylated type I collagen, in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, comprising the method steps a) providing an expression system which has at least one expression cassette, wherein the expression cassette has at least one nucleotide sequence which has a type I Collagen, in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, encoded and wherein the expression system is capable of hydroxylating proline, lysine or proline and lysine residues of the expressed collagen peptide, b) culturing the expression system under conditions that allow the expression and hydroxylation of type I collagen, in particular type I collagen peptide, c) obtaining the type I collagen according
  • the recombinant in vivo hydroxylated collagen peptide produced according to the invention has a biological activity.
  • the expression system provided in step a) is an expression system which is incapable of causing hydroxylation of proline, lysine or proline and lysine residues of the expressed collagen peptide, in particular that has in step a) provided expression system no prolyl hydroxylase and lysyl hydroxylase activity.
  • the present invention thus includes a method for producing a recombinant collagen peptide that can be used according to the invention, in particular a non-hydroxylated collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, comprising the method steps a) providing an expression system which has at least one expression cassette, wherein the expression cassette has at least one nucleotide sequence which encodes a type I collagen, in particular type I collagen peptide, with a molecular weight of at least 16 kDa, in particular at least 20 kDa, and wherein the Expression system is not capable of hydroxylating proline, lysine or proline and lysine residues of the expressed type I collagen, in particular type I collagen peptide, b) culturing the expression system under conditions that the expression of type I collagen, in particular type I collagen peptides, allow c) obtaining the type I collagen according to the invention, in particular type I collagen peptide, in particular the non
  • the at least one nucleotide sequence of the at least one expression cassette is codon-optimized, which means that those codons in the nucleotide sequence that are not or are not preferably used are replaced by those that are preferably used by the translation system of the provided expression system, in particular the provided cell-based expression system, in particular the provided host cell, without thereby changing the amino acid sequence of the encoded peptide or protein.
  • the type I collagen, in particular type I collagen peptide, encoded by the nucleotide sequence is a type I collagen, in particular type I collagen peptide, of a vertebrate, in particular a mammal, e.g. human, or not - a human mammal, e.g. horse, kangaroo, rodent, pig, ovine or bovine, a bird, e.g. chicken, a fish, an amphibian, a reptile or an invertebrate, e.g. jellyfish.
  • the expression cassette provided in step a) comprises at least one nucleotide sequence according to SEQ ID No. 1, 3, 5 or 7.
  • the expression cassette provided in step a) comprises at least one nucleotide sequence with a sequence identity of at least 90%, preferably at least 95%, preferably at least 96%, preferably at least 97%, preferably at least 98%, preferably at least 99%, to the nucleotide sequence according to SEQ ID No. 1, 3, 5 or 7.
  • the type I collagen encoded by the nucleotide sequence, in particular type I collagen peptide is a type I collagen, in particular type I collagen peptide, comprising the amino acid sequence according to SEQ ID No. 2, 4, 6 or 8
  • Type I collagen encoded by the nucleotide sequence, in particular type I collagen peptide from the amino acid sequence according to SEQ ID No. 2, 4, 6 or 8.
  • the type I collagen encoded by the nucleotide sequence in particular type I collagen peptide, has at least 80%, preferably at least 85%, preferably at least 90%, preferably at least 95%, preferably at least 96% at least 97%, preferably at least 98%, preferably at least 99% sequence identity with the amino acid sequence according to SEQ ID No. 2, 4, 6 or 8.
  • the type I collagen, in particular type I collagen peptide, encoded by the nucleotide sequence is a naturally occurring type I collagen, in particular type I collagen peptide.
  • the type I collagen, in particular type I collagen peptide, encoded by the nucleotide sequence is not a naturally occurring type I collagen, in particular type I collagen peptide.
  • the type I collagen encoded by the nucleotide sequence, in particular type I collagen peptide is preferably a genetically modified collagen peptide.
  • the at least one nucleotide sequence encodes a type I collagen peptide having a molecular weight in a range from 16 to 400 Da, in particular 16 to 390 kDa, in particular 16 to 350 kDa, in particular 16 to 300 kDa, in particular 16 to 110 kDa, in particular 20 to 400 kDa, in particular 20 to 390 kDa, in particular 20 to 350 kDa, in particular 20 to 300 kDa, in particular 20 to 110 kDa, in particular 40 to 110 kDa, in particular 40 to 100 kDa, in particular 21 to 105 kDa , in particular 80 to 100 kDa, in particular 25 to 100 kDa, in particular 20 to 99 kDa, in particular 20 kDa, in particular 25 to 95 kDa, in particular 30 to 95 kDa, in particular 35 to 95 kDa, in particular 92 kDa, in particular from 40 to 50
  • the methods according to the invention are distinguished in that in method step b) conditions are selected which enable the formation of a triple-helical form of type I collagen, in particular type I collagen peptides.
  • the methods according to the invention can lead to the production of homogeneous and isolated preparations of specific type I collagen peptides with a uniform molecular weight.
  • the invention also provides mixtures of isolated and homogeneous preparations of type I collagen peptides produced in this way, each with a uniform molecular weight.
  • the invention also envisages providing recombinant collagen peptide hydrolyzates by lysis, in particular hydrolysis, from type I collagen peptides which are produced by means of the method according to the invention and are optionally present homogeneously and in isolation and have a uniform molecular weight.
  • the present invention provides in particular for providing both the homogeneously isolated type I collagen peptides with a uniform molecular weight, their mixtures or their hydrolyzates for the oral therapy of inflammatory skin and mucous membrane diseases of a human or animal body provided according to the invention.
  • the methods according to the invention are characterized in that following method step b) or c) in a method step d) in a by lysis, in particular hydrolysis, of the expressed type I collagen, in particular type I collagen peptide, a type I - collagen peptide hydrolyzate is obtained.
  • the type I collagen peptide hydrolyzate obtained according to the invention by process step d) can be used as the type I collagen peptide according to the invention either in the form of this type I collagen peptide hydrolyzate or after isolation of one or more type I collagen peptides, preferably present homogeneously and isolated.
  • homogeneous and isolated type I collagen peptides are mixed with one another and thus represent a mixture of type I collagen peptides, all type I collagen peptides having a molecular weight of at least 16 kDa, in particular at least 20 kDa.
  • the invention therefore also relates to a type I collagen peptide which is present in an isolated, homogeneous form with a uniform molecular weight, or a type I collagen peptide which is in a mixture with recombinant or natural, in particular recombinant type I collagen peptides is present, or is present in a hydrolyzate of a recombinant type I collagen, in particular a recombinant type I collagen peptide.
  • nucleotide sequences which can be used according to the invention and which code for the recombinant type I collagen peptide can be obtained in a manner customary in the art, for example as described in WO 2005/012356, WO 01/34646, WO 01/34647 and WO 01/34801.
  • the type I collagen, in particular type I collagen peptide which can be used according to the invention and is preferably produced using one of the aforementioned methods according to the invention, having a molecular weight of at least 16 kDa, in particular at least 20 kDa, is for use in a method for the therapeutic treatment of inflammatory skin and mucous membrane diseases of the human or animal body, a non-hydroxylated, partially hydroxylated or fully hydroxylated type I collagen peptide, preferably a non-hydroxylated type I collagen peptide, preferably a partially hydroxylated type I collagen peptide, preferably a fully hydroxylated type I collagen peptide.
  • the type I collagen in particular natural or recombinant type I collagen peptide, which can be used according to the invention and is preferably produced using one of the above methods, has a molecular weight of at least 16 kDa, in particular at least 20 kDa, for use in a method for the therapeutic treatment of inflammatory skin and mucous membrane diseases of the human or animal body, a glycosylated collagen peptide.
  • the type I collagen, in particular type I collagen peptide is preferably glycosylated in vivo, preferably glycosylated ex vivo.
  • type I collagen in particular type I collagen peptide
  • a non-glycosylated type I collagen in particular type I collagen peptide
  • biological activity is preferably understood to mean the ability of the type I collagens that can be used according to the invention, in particular type I collagen peptides, to immunomodulate, in particular to regenerate immunosuppressive M2 macrophages, in particular from peripheral monocytes, and/or regenerate immunosuppressive T Suppressor cells, especially from T-progenitor cells.
  • biological effectiveness is preferably understood according to the invention as the ability of the type I collagens that can be used according to the invention, in particular type I collagen peptides, the formation and activity of pro-inflammatory cytokines, in particular TNFa, IL-6, IL-lß and IFN ⁇ , to suppress or to stimulate the synthesis and activity of anti-inflammatory cytokines, in particular IL-4, IL-10 and TGF- ⁇ , in particular in dem.
  • the term "biological activity” is preferably understood to mean that the type I collagens that can be used according to the invention, in particular type I collagen peptides, for immunomodulation, in particular for the regeneration of immunosuppressive M2 macrophages, in particular from peripheral monocytes, and/or for the regeneration of immunosuppressive T - Suppressor cells, in particular from T-progenitor cells, to suppress the formation of proinflammatory cytokines, in particular TNFa, IL-6, IL-lß and IFNy, and to stimulate the synthesis of anti-inflammatory cytokines, in particular IL-4, IL- 10 and TGF-ß.
  • the biological effectiveness is determined in particular by means of detection methods familiar to the person skilled in the art for immunomodulating, in particular stimulating and suppressing, activities of substances and for anti-inflammatory and pro-inflammatory cytokines.
  • the biological activity for the purposes of the present invention is determined using the procedure according to Examples 2 to 4.
  • the term “biological activity” preferably also includes the induction ability of the type I collagens that can be used according to the invention, in particular type I collagen peptides understanding of oral tolerance.
  • the presence of oral tolerance is determined by means of detection methods familiar to the person skilled in the art for determining the ability of a substance to induce oral tolerance, in particular by means of the procedure according to Examples 2 to 4.
  • pro-inflammatory cytokines are in particular TNF ⁇ , IL-6, IL-1 ⁇ and IFN-gamma (JFN ⁇ ).
  • anti-inflammatory cytokines are in particular IL-4, IL-10 and TGF- ⁇ .
  • suppression is understood to mean the partial or complete suppression of a synthesis of proteins, which can present itself in particular as a reduction or inhibition of protein synthesis or as a reduction or inhibition of the mRNA synthesis affecting the proteins.
  • the term “collagen” is understood in a manner customary in the art, in particular as defined, for example, in WO 01/34646.
  • the term “collagen” refers to a collagen protein having the sequence glycine-proline, glycine-4-hydroxyproline or glycine-X-4-hydroxyproline, preferably the repetitive motif (Gly-X-Y)n Understood peptide, where X and Y can be any amino acid, preferably proline and 4-hydroxyproline are.
  • the term “collagen” particularly preferably means a peptide having the repetitive motif (Gly-Pro-Y)n and/or (Gly-X-Hyp)m, where X and Y can be any amino acid.
  • a “type I collagen” according to the present invention is a collagen as is understood in the art according to the above statements, wherein the type I collagen has the amino acid sequence of a naturally occurring type I collagen, in particular the amino acid sequence of a type I collagen of a vertebrate, in particular pig, sheep, bovine, rodent, horse, bird, fish, reptile or amphibian or an invertebrate, in particular jellyfish.
  • the type I collagen can be present as a monomeric collagen peptide, also referred to here as a single-stranded collagen peptide, or as a dimer or trimer, in particular trimer, having at least two, in particular three collagen peptides, from in particular different or the same single-stranded collagen peptides.
  • the type I collagen can be present as a triple-helical type I collagen peptide, in particular native type I collagen.
  • type I collagen peptide means a single-stranded type I collagen peptide which has an amino acid sequence occurring in type I collagen as defined above, the peptide being an oligopeptide or polypeptide .
  • the type I collagen peptide can in particular in chemically modified form, in particular hydroxylated and/or glycosylated form, or be unmodified.
  • the recombinant type I collagen used according to the invention in particular type I collagen peptide, can preferably have a sequence modification, in particular a function-preserving sequence modification of a naturally occurring type I collagen, in particular type I collagen peptide.
  • a "type I collagen” is also understood to mean a functionally-preserving sequence modification of a naturally occurring type I collagen, in particular type I collagen peptides, in particular if this has an amino acid sequence identity of at least 80% to the amino acid sequence of the naturally occurring type I collagen at the amino acid level occurring type I collagen have, in particular at least 85%, in particular at least 90%, in particular at least 95%, in particular at least 96%, in particular at least 97%, in particular at least 98%, in particular at least 99% amino acid sequence identity.
  • a type I collagen is present when the recombinant type I collagen either has exactly the amino acid sequence that occurs in a naturally occurring type I collagen or when a functional sequence modification with an amino acid sequence identity of at least 80% is at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% over a naturally occurring type I collagen , in particular to naturally occurring type I collagen from a vertebrate, in particular pig, sheep, bovine, rodent, kangaroo, horse, a bird, a reptile, an amphibian or a fish or an invertebrate, in particular jellyfish, is present, in particular if this amino acid - identity to a naturally occurring bovine type I collagen amino acid sequence.
  • amino acid sequence identity is determined using the Smith-Waterman algorithm (SSE2, Michael Farrar, 2006, 7.2 November 2010) with the parameters BL50 matrix (15:-5), Open/ext: -12 /-2, determined.
  • function-preserving sequence modification is understood according to the invention as the modification of a given, in particular naturally occurring, amino acid sequence, in particular the replacement, addition and / or deletion of one or more amino acids, which leads to an amino acid sequence deviating from the given amino acid sequence, which modified amino acid sequence, however, for the given amino acid sequence characteristic function, in particular their biological effectiveness, retained.
  • a “function-preserving sequence modification” is preferably understood as meaning a modification of a given, in particular naturally occurring, amino acid sequence in which the function characteristic of the given amino acid sequence, in particular a biological effectiveness, is at least 50%, preferably at least 60%, preferably at least 70%, preferably at least 80%, preferably at least 90%, preferably at least 95%, preferably 100% is maintained.
  • a “function-preserving sequence modification” is understood as meaning a modification of a given amino acid sequence in which the modified amino acid sequence accounts for at least 50%, preferably at least 55%, preferably at least 60%, preferably at least 65%, preferably at least 70%, preferably at least 75% , preferably at least 80%, preferably at least 85%, preferably at least 90% sequence homology to the given amino acid sequence.
  • sequence modification in particular a "function-preserving sequence modification" in connection with the present invention, a modification of a given, in particular naturally occurring amino acid sequence, in which one or more amino acids with certain chemical-physical properties are replaced by one or more amino acids with the same or similar ones chemical-physical properties have been replaced, in particular, for example, an amino acid with a non-polar side chain (e.g. Ala, Val, Met, Leu, Ile, Pro, Trp, Phe) by another amino acid with a non-polar side chain (e.g. Ala, Val, Met, Leu , Ile, Pro, Trp, Phe), an amino acid with a polar neural side chain (e.g.
  • a non-polar side chain e.g. Ala, Val, Met, Leu, Ile, Pro, Trp, Phe
  • an amino acid with a polar neural side chain e.g.
  • sequence modification in particular a "function-preserving sequence modification”
  • a sequence modification in particular a "function-preserving sequence modification” is also understood to mean the modification of a given amino acid sequence, in particular a naturally occurring amino acid sequence, which consists in the given amino acid sequence, in particular the naturally occurring amino acid sequence, containing at least one amino acid, preferably at least one essential one Amino acid, in particular Ile, Leu, Lys, Met, Phe, Thr, Trp, Val, His, Cys, Tyr, particularly preferably Trp, was added, the function characteristic of the given amino acid sequence, in particular the naturally occurring amino acid sequence, in particular the biological effectiveness of the present invention, in particular the biological effectiveness according to the evidence presented in Example 2, is retained.
  • the at least one amino acid preferably the at least one essential amino acid, in particular Ile, Leu, Lys, Met, Phe, Thr, Trp, Val, His, Cys, Tyr, particularly preferably Trp, N-terminal, C - add terminally and/or within the amino acid sequence.
  • amino acid modification refers to a chemical modification of one or more amino acids that may have taken place before, after or during the synthesis of the recombinant type I collagen, in particular type I collagen peptide, while retaining the original amino acid backbone, in particular one or more proteinogenic amino acids, the type I collagen peptide.
  • the term includes both the use of chemically modified amino acids for the synthesis of the type I collagen according to the invention, in particular type I collagen peptide, and the chemical modification of the amino acids after or during the synthesis of the type I collagen, particularly type I collagen peptides.
  • Amino acid modifications typical of collagen peptides are, in particular, hydroxylations on proline and lysine residues and glycosylation of hydroxylated lysine residues. According to the invention, however, the term also includes other chemical modifications of amino acids, such as phosphorylation, N-glycosylation, acetylation, methylation or myristoylation.
  • a recombinant type I collagen, in particular type I collagen peptide, or a recombinantly produced type I collagen, in particular type I collagen peptide is a type I collagen obtained by biotechnological recombinant production using an expression system , especially type I collagen peptide understood.
  • the recombinant type I collagen, in particular type I collagen peptide, or the recombinantly produced type I collagen, in particular type I collagen peptide have in common that they are not obtained from natural sources.
  • the recombinant type I collagen in particular type I collagen peptide
  • only type I collagens or type I collagen peptides of a certain specific size, ie a certain molecular weight are present in a homogeneous preparation, ie a single molecular species, in particular with the identical amino acid sequence.
  • the recombinant type I collagen or the type I collagen peptide is in isolated form.
  • the recombinant type I collagen or the type I collagen peptide is free from other proteins or peptides, in particular free from other substances, for example impurities, in particular free from non-protein material, free from salts and /or free from other proteins or peptides.
  • the natural type I collagen in particular type I collagen peptide
  • only type I collagens or type I collagen peptides of a certain specific size, ie a certain molecular weight are present in a homogeneous preparation, ie a single molecular species, in particular with the identical amino acid sequence.
  • the natural type I collagen or the type I collagen peptide is present in isolated form.
  • the natural type I collagen or the type I collagen peptide is free from other proteins or peptides, in particular free from other substances, for example impurities, in particular free from non-protein material, free from salts and /or free from other proteins or peptides.
  • the natural type I collagen or the type I collagen peptide with a molecular weight of at least 16 kDa is free of collagen, in particular also free of collagen peptides, with a molecular weight of less than 16 kDa.
  • the molecular weight is preferably determined by means of gel permeation chromatography.
  • the term “gelatin” is understood in a manner customary in the art, in particular as defined, for example, in WO 01/34646.
  • the term “recombinant DNA” refers to an artificially produced or manipulated DNA molecule that was produced in vitro using genetic engineering methods.
  • the recombinant DNA is composed of components from different organisms of origin.
  • the term "expression cassette" means a DNA segment that is responsible for the transcription of the information encoded in this segment into an RNA, in particular into an mRNA, and at least one promoter and one protein-coding nucleotide sequence, in usually has at least one promoter, at least one protein-coding nucleotide sequence and optionally a terminator.
  • nucleotide sequence is understood to mean the sequence, in particular a continuous sequence, of the nucleotides of a nucleic acid, in particular a nucleic acid strand, in particular a DNA or RNA strand.
  • a "nucleotide sequence” is therefore to be understood both as an informational unit and as the DNA or RNA strand that physically manifests this information.
  • an “expression system” means a system in which a targeted and controlled protein biosynthesis can take place.
  • the term "expression system” according to the invention includes both cell-free expression systems in which the components required for protein biosynthesis are not present within a cell, i.e. the protein biosynthesis takes place outside of a cell, and cell-based expression systems in which the protein biosynthesis takes place within a living cell.
  • a cell-free expression system is preferably a lysate or an extract from E. coli, insect cells, wheat germs, tobacco cells or mammalian cells, in particular CHO cells or reticulocytes from rabbits, which contains the components necessary for protein biosynthesis, in particular a translation and a transcription system.
  • the term “culturing” is synonymous with "incubating”.
  • a “host cell” is understood to mean a living cell which is capable of expressing peptides or proteins encoded in foreign DNA, in particular in recombinant DNA.
  • the term “obtaining type I collagen, in particular type I collagen peptide”, according to process step c) describes a method known to the person skilled in the art for isolating type I collagen or type I collagen peptide from a composition containing several components by means of known isolation methods , such as centrifugation methods, in particular differential centrifugation and/or Density gradient centrifugation, chromatographic methods, in particular gel filtration, ion exchange, affinity and/or high-performance liquid chromatography, electrophoresis methods, filtration methods and/or extraction methods, understood, wherein an enrichment and purification of the component concerned from the composition containing several components is preferably achieved by sequential application of several isolation methods can be. If appropriate, C- and/or N-terminal procollagen fragments can be cleaved off before, after or during the extraction in order to obtain collagen.
  • isolation methods such as centrifugation methods, in particular differential centrifugation and/or Density gradient centrifugation, chromatographic methods, in particular gel filtration,
  • Fibrillogenesis chemical modifications and secretion of the expressed type I collagen peptide can preferably also take place under the conditions of method step b).
  • condition that enable the expression of type I collagen, in particular type I collagen peptide allow” to be understood as meaning conditions such as, in particular, temperature, pressure, time, light and the presence or absence of inducers and/or repressors Activate or enhance expression of type I collagen, particularly type I collagen peptide.
  • the type I collagen, in particular type I collagen peptide is expressed in the context of a high cell density fermentation, in particular under high pressure, preferably high air pressure.
  • the specific conditions which allow expression of the type I collagen, in particular type I collagen peptide are known to the person skilled in the art and depend on the expression system used and the expression cassette used, in particular the promoter contained therein. Depending on the structure of the expression cassette, expression of type I collagen, in particular type I collagen peptide, can be constitutive or inducible.
  • a therapeutic method for the oral therapy of “inflammatory skin and mucosal diseases” is a method for the prevention and/or treatment of inflammatory skin and mucosal diseases, in particular for the treatment of immune-modulated inflammatory skin and mucosal diseases, in particular intestinal mucosal diseases , Understood, the administration of the type I collagen is carried out orally.
  • Inflammatory skin and mucous membrane diseases in the context of the present invention are in particular skin and mucous membrane diseases, in particular of the skin, caused by autoimmune reactions, in particular by excessive immune reactions.
  • autoimmune reactions in particular by excessive immune reactions.
  • a therapeutic method for the oral therapy of “inflammatory skin and mucous membrane diseases” also includes a method for inducing oral tolerance to endogenous collagen, in particular endogenous type I collagen, in particular endogenous type I collagen present in or on skin or mucous membrane tissue , understood.
  • immunomodulated inflammatory skin and mucosal diseases are understood to mean that the inflammatory skin and mucosal diseases are caused completely or at least partially by autoimmune diseases and/or immune intolerance, in particular to collagen type I.
  • the terms “comprising” and “having” mean that in addition to the elements explicitly covered by these terms, other elements that are not explicitly mentioned can also occur. In connection with the present invention, these terms also mean that only the elements explicitly mentioned are covered and no further elements are present. In this particular embodiment, the meaning of the terms “comprising” and “comprising” is synonymous with the term “consisting of”. In addition, the terms “comprising” and “having” also include compositions that, in addition to the elements explicitly mentioned, also contain other elements that are not mentioned, but which are of a functionally and qualitatively subordinate nature. In this embodiment, the terms “comprising” and “comprising” are synonymous with the term “consisting essentially of”.
  • the first and second decimal place or the second decimal place are/is not specified, they are/is to be set as 0.
  • SEQ ID No. 1 The coding nucleotide sequence of a 16 kDa bovine type I recombinant collagen peptide (CP16) (type COL1A1;).
  • SEQ ID No. 2 The amino acid sequence of the collagen peptide according to SEQ ID No. 1.
  • SEQ ID No. 3 The coding nucleotide sequence of a 20 kDa bovine type I recombinant collagen peptide (CP20) (type COLI A1).
  • SEQ ID No. 4 The amino acid sequence of the collagen peptide according to SEQ ID No. 3.
  • SEQ ID No. 5 The coding nucleotide sequence of a 45 kDa bovine type I recombinant collagen peptide (CP45) (type COLI A1).
  • SEQ ID No. 6 The amino acid sequence of the collagen peptide according to SEQ ID No. 5.
  • SEQ ID No. 7 The coding nucleotide sequence of a 92 kDa bovine type I recombinant collagen peptide (CP90) (type COLI A1).
  • SEQ ID No. 8 The amino acid sequence of the collagen peptide according to SEQ ID No. 7.
  • SEQ ID NO:9 The amino acid sequence of a control 8 kDa (7912 Da) hydroxylated bovine collagen peptide (hereinafter CP9).
  • Figures 1 to 11 show in graphic form the stimulation or inhibition of the formation of anti- and pro-inflammatory cytokines and the surface marker CD86 in M2 macrophages ( Figures 1 and 2), differentiated macrophages ( Figures 3 and 4), T suppressor cells ( Figures 5 to 8) and dermal fibroblasts ( Figures 9 to 11).
  • Example 1 Production of recombinant type I collagen
  • Recombinantly produced hydroxylated bovine collagen peptides of type I with the designations CP 16, CP20, CP45 and CP90 and with the amino acid sequences according to SEQ ID Nos. 2, 4, 6 and 8 were, by recombinant expression, the nucleotide sequence according to SEQ ID Nos. 1, 3, 5 or 7 expression cassette in a Komagataella phaffi strain capable of hydroxylating proline residues.
  • an experimental control was provided in the form of the collagen peptide CP9 (SEQ ID No. 9) known from WO 2020/127929.
  • strains used in each case for the recombinant expression of the collagen peptides were obtained by genomic integration of the coding nucleotide sequences of the respective bovine type I collagen peptides or the coding nucleotide sequence of a monomeric prolyl-4-hydroxylase from the Mimivirus (P4H).
  • Example 2 Proof of effectiveness - immune and cytokine modulation by type I collagen peptides according to example 1
  • the inner layer of the gut consists of mucoid fluid-secreting enterocytes and an underlying lamina muscular tract of loose connective tissue.
  • the mucosa is infiltrated by gut-associated lymphoid tissue (GALT), which is part of the immune system and is involved in protecting the body from pathogens entering the gut.
  • GALT gut-associated lymphoid tissue
  • the GALT consists of mesenteric lymph nodes of lymphoid tissue called Peyer's patches.
  • the lymphoid follicles are surrounded by an epithelial layer and specialized microfolded M cells, which are characterized by a reduced microvilli border and a glycocalyx and are exposed to the inner gut.
  • M cells specialize in taking up macromolecules such as soluble proteins, peptides, commensal and pathogenic microorganisms and viruses. Peyer's patches recognize and evaluate these macromolecules after transcytosis. Depending on the antigen compound, they turn the body's immune response on or off. pathogens are delivered to mononuclear phagocytes and lymphocytes located in the basolateral membrane of M cells.
  • Native type I collagen is recognized by Peyer's patches via its "active" epitopes and the additional glycopeptide side chains of the collagens.
  • Native type I collagen activates macrophages and dendritic cells, which then activate T cell progenitors in the lymphatic follicles to specify into type I collagen regulatory T cells.
  • Mature T cells then enter the bloodstream via the thoracic duct and, after reaching the target tissue, release mediators that stimulate the immune response in the tissue by releasing anti-inflammatory cytokines, IL-10, IL-4 and TGF-ß. weaken.
  • the pro-inflammatory cytokine TNF- ⁇ will be downregulated in the target tissue.
  • the immunomodulatory effect of the recombinantly produced type I collagen peptides according to Example 1 was determined in human peripheral blood monocytes (PBMC).
  • PBMC peripheral blood monocytes
  • 3H10-25 commercially available cells from 3H-Biomedical AB, (Sweden) were used.
  • the PBMC cells were first cultivated in macrophage base medium DXF (C-28057, PromoCell, Germany) in cell culture flasks coated with human fibronectin (C-43060, PromoCell, Germany).
  • the culture medium was supplemented with the associated supplement mix (supplement to C-28055, PromoCell, Germany) and with 1% amphotericin and 1% penicillin-streptomycin.
  • a polarization of the adherent monocytes to immunosuppressive type 2b or 2c macrophages was induced by the addition of 4 pg/mL recombinant type I collagen.
  • the cells were each incubated for 6 days with the samples to be examined.
  • the macrophages activated in this way were then polarized by adding 1 pg/mL lipopolysaccharides from Escherichia coli (LPS, L6529, Merck, Germany).
  • the differentiation pattern of the generated macrophages was examined using specific cell differentiation markers (CDs).
  • CDs cell differentiation markers
  • the differentiation of the monocytes into inflammation-inducing M1 macrophages or into immunosuppressive M2 macrophages was demonstrated using specific markers.
  • the M2 surface markers CD86, CD14 and CD163 were determined using ELISA (“enzyme-linked immunosorbent assay”). The respective detections were carried out for CD86 (850590096 Diaclone, Hölzel Diagnostics, Germany), CD14 (850780096 Diaclone, Hölzel Diagnostics, Germany) and CD 163 (ELH-CD163 RayBiotech, Hölzel Diagnostics) exactly according to the manufacturer's instructions.
  • Ml macrophage markers CD86 850590096 Diaclone, Hölzel Diagnostics, Germany
  • CD80 EK0707 Boster PicoKine, Hölzel Diagnostics, Germany
  • TNFa pro-inflammatory
  • JFNy pro-inflammatory
  • IL-10 anti-inflammatory cytokines
  • IFNY IFNY
  • the differentiation of the monocytes into M1 or M2 macrophages was checked using a special differentiation medium (C-28055, PromoCell, Germany) and specific cultivation additives.
  • a special differentiation medium C-28055, PromoCell, Germany
  • the monocytes were cultured with macrophage differentiation medium (C-28055, PromoCell, Germany), to which a GM-CSF supplementation mix (C60420A, PromoCell, Germany) was added to indicate M1 differentiation, or for M2 differentiation M-CSF GM-CSF supplementation mix (C60442A, PromoCell, Germany) were added.
  • the synthesis profile of the cytokines showed an anti-inflammatory effect of the investigated type I collagen peptides.
  • the synthesis of inflammatory cytokines was suppressed and the synthesis of anti-inflammatory IL-10 was induced.
  • Example s Proof of effectiveness - stimulation of na ⁇ ve CD4 + T progenitor cells by type I collagen peptides according to example 1
  • the macrophage base medium DXF (C-28057, PromoCell, Germany) was compared to T cell culture medium (3H800-50-50 , 3H Biomedical AB, Sweden).
  • T cell culture medium 3H800-50-50 , 3H Biomedical AB, Sweden.
  • na ⁇ ve CD4 + T progenitor cells 3H31-k, 3H Biomedical AB, Sweden).
  • the T progenitor cells differentiate into collagen-specific (CP90, CP45, CP20 or CP16) regulatory T suppressor cells.
  • the mature T-suppressor cells were enriched using the ARTE (antigen-reactive T-cell enrichment) method, since specific T-cell clones are formed only with a low frequency.
  • the specificity of the T cells is determined by labeling the cells with cell surface marker (CD) antibodies coupled to various dyes such as biotin or phycoerythrin, followed by anti-biotin and anti-PE MicroBeads.
  • CD cell surface marker
  • the magnetic MicroBeads are used to separate and collect specific T cell clone types. Subsequently, the T cells can be stained with fluorochrome-conjugated antibodies and quantified using flow cytometry.
  • T suppressor cells are identified by Forkhead Box p3 (FoxP3) and CD25.
  • T suppressor cells After their differentiation, T suppressor cells release an anti-inflammatory cytokine cocktail of IL-10, IL-4 and TGF-ß.
  • the data obtained showed a statistically significant, advantageous effect of the tested collagen peptides CP90, CP45, CP20 and CP16 for the regeneration of immunosuppressive T-suppressor cells.
  • T-suppressor cells The differentiation of T-suppressor cells was demonstrated by the expression of forkhead box p3 (FoxP3).
  • FIGS. 5 to 8 The investigations according to FIGS. 5 to 8 were carried out on T suppressor cells.
  • Human, dermal fibroblasts were cultivated in Hams-F12 medium (HAM-12-A, Capricorn, Germany) mixed with 1% amphotericin and with 1% penicillin-streptomycin and 10% calf serum. After reaching 100 percent cell confluence, an inflammatory situation was induced in the fibroblasts by adding 1 pg/ml lipopolysaccharides (Escherichia coli, L6529, Merck, Germany). The addition of 25 ⁇ l/ml cell supernatant from the T-cell differentiation experiment (Example 3) reduced the inflammation in the dermal fibroblasts.

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Abstract

La présente invention concerne un collagène de type I recombinant, en particulier non dénaturé, destiné à être utilisé dans un procédé thérapeutique pour la thérapie par voie orale de maladies inflammatoires de la peau et des muqueuses chez un patient humain ou animal.
EP22844043.4A 2021-12-22 2022-12-21 Peptide de collagène de type i à usage thérapeutique Pending EP4452301A1 (fr)

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US5637321A (en) 1994-02-28 1997-06-10 Moore; Eugene R. Method for preparing animal tissue for use in alleviating the symptoms of arthritis in mammals
US5750144A (en) 1994-02-28 1998-05-12 Moore; Eugene R. Method for alleviating the symptoms of arthritis in mammals
US5645851A (en) 1994-02-28 1997-07-08 Moore; Eugene R. Product for alleviating the symptons of arthritis in mammals
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WO1996021458A1 (fr) * 1995-01-10 1996-07-18 Fibrogen, Inc. Methodes et formulations a base de collagene pour le traitement de maladies d'origine immunologique
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US20050058703A1 (en) 2003-08-01 2005-03-17 Chang Robert C. Gelatin capsules
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US9095569B2 (en) * 2008-04-18 2015-08-04 Collplant Ltd. Methods of generating and using procollagen
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